Design,synthesis and biological evaluation of novel Fluoroquinolone derivatives as potential,selective inhibitors of PI3Kγ
Phosphoinosilide 3-kinase(PI3K) is an attractive target to potentially treat a range of disease stales as illustrated by more than 15 inhibitors now in clinical trials.We disclose herein the discovery of a new class of fluoroquinolone derivatives having improved potency toward PI3K.
Shao Sha Hong-Wei Han Fei Gao Tian-Bao Liu Zhen Li Chi Xu Wei-Qing Zhong Hai-Liang Zhu
State Key Laboratory of Pharmaceutical Biotechnology,Nanjing University,Nanjing 210093,PR China School of Pharmacy,Second Military Medical University,Shanghai 200433,P.P.China State Key Laboratory of Pharmaceutical Biotechnology,Nanjing University,Nanjing 210093,PR China;Scho
国内会议
大连
英文
331-331
2016-09-24(万方平台首次上网日期,不代表论文的发表时间)